Canonical Allele Identifier: CA900676826

Gene: CLRN1

Linked Data

• dbSNP Id: rs1454755989
• gnomAD v3: 3-150941933-G-A
• gnomAD v4: 3-150941933-G-A
• MyVariant Identifiers: chr3:g.150659720G>A (hg19) ; chr3:g.150941933G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.150941933G>A , CM000665.2:g.150941933G>A	GRCh38
NC_000003.11:g.150659720G>A , CM000665.1:g.150659720G>A	GRCh37
NC_000003.10:g.152142410G>A	NCBI36
NG_009168.1:g.36067C>T , LRG_700:g.36067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327047.6:c.254-172C>T MANE Select	ENSP00000322280.1:n.254-172C>T
ENST00000468836.2:c.402-172C>T	ENSP00000419892.2:n.402-172C>T
ENST00000644099.1:c.246-172C>T	ENSP00000494762.1:n.246-172C>T
ENST00000295911.6:c.26-172C>T	ENSP00000295911.2:n.26-172C>T
ENST00000327047.5:c.254-172C>T	ENSP00000322280.1:n.254-172C>T
ENST00000328863.8:c.254-172C>T	ENSP00000329158.4:n.254-172C>T
ENST00000468836.1:c.26-172C>T	ENSP00000419892.1:n.26-172C>T
ENST00000472224.1:n.260-172C>T
ENST00000485607.1:c.-83-172C>T	ENSP00000419244.1:n.-83-172C>T
NM_001195794.1:c.254-172C>T , LRG_700t1:c.254-172C>T	NP_001182723.1:n.254-172C>T
NM_001256819.1:c.426-172C>T	NP_001243748.1:n.426-172C>T
NM_052995.2:c.26-172C>T , LRG_700t2:c.26-172C>T	NP_443721.1:n.26-172C>T
NM_174878.2:c.254-172C>T	NP_777367.1:n.254-172C>T
NR_046380.2:n.696-172C>T
XR_924167.1:n.566-172C>T
NM_001256819.2:c.426-172C>T	NP_001243748.1:n.426-172C>T
NM_174878.3:c.254-172C>T MANE Select	NP_777367.1:n.254-172C>T
NR_046380.3:n.424-172C>T